A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796349



Internal ID21241687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89536470..89536470hg38UCSC Ensembl
chr16:89602878..89602878hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677086
Samples
Known GenesSPG7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796349
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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